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HRID 2398964作成日:2026年10月25日

Isobutyl chloroformate → 8-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

https://huagongshe.com/reaction/2398964

反応式

関与物質

役割名称HCID仕込み量
反応物Isobutyl chloroformateHCID 62365—
反応物7-Amino-3-{[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 3149822—
反応物p-ChloromethylphenylglycineHCID 22767740—
溶媒TriethylamineHCID 8471—
生成物8-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 19091993—

反応手順

p-Chloromethylphenylglycine wherein the amino group is protected with tert-butoxycarbonyl is treated with isobutylchloroformate in the presence of triethylamine. The thus obtained anhydride is reacted with the triethylamine salt of 3-[(2-methyl-1,3,4-thiadiazol-5-ylthio)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid at 0° C. for about 4 hours.The resulting product is isolated, and the amine protecting group is removed by acid hydrolysis to give 3-[(2-methyl-1,3,4-thiadiazol-5-ylthio)methyl]-7-[[2-[4-chloromethyl)phenyl]-2-aminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04026887
出典データセットuspto-grants-1977_05
ORD IDord-414e91285bcc45d6883b4cd3486af122
出典メモuspto-grants-1977_05